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2,4-Dinitrophenylhydrazone mesityl oxide

Base Information
  • Chemical Name:2,4-Dinitrophenylhydrazone mesityl oxide
  • CAS No.:964-83-0
  • Molecular Formula:C12H14N4O4
  • Molecular Weight:278.268
  • Hs Code.:
  • NSC Number:404137
  • DSSTox Substance ID:DTXSID20429835
2,4-Dinitrophenylhydrazone mesityl oxide

Synonyms:2,4-dinitrophenylhydrazone mesityl oxide;964-83-0;NSC404137;DTXSID20429835;STK524799;AKOS001011421;NSC-404137;SR-01000033371;SR-01000033371-1;Z56834202;(2E)-1-(2,4-dinitrophenyl)-2-(4-methylpent-3-en-2-ylidene)hydrazine

Suppliers and Price of 2,4-Dinitrophenylhydrazone mesityl oxide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 7 raw suppliers
Chemical Property of 2,4-Dinitrophenylhydrazone mesityl oxide
Chemical Property:
  • Vapor Pressure:7.86E-07mmHg at 25°C 
  • Boiling Point:406.9°C at 760 mmHg 
  • Flash Point:199.9°C 
  • Density:1.29g/cm3 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:278.10150494
  • Heavy Atom Count:20
  • Complexity:432
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=CC(=NNC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-])C)C
  • Isomeric SMILES:CC(=C/C(=N/NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-])/C)C
Technology Process of 2,4-Dinitrophenylhydrazone mesityl oxide

There total 11 articles about 2,4-Dinitrophenylhydrazone mesityl oxide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1: 87 percent / p-toluenosulfonic acid / 1.) o deg C, 30 min., 2.) room temp., overnight
2: 4.5 g / p-toluenesulfonic acid / Heating
3: 76 percent / potassium t-butoxide / pentane / 1.) 0 deg C, 30 min., 2.) 2 h, room temp.
4: MeLi / diethyl ether / 1.) 0 deg C, 0.5 h, 2.) 2 h, room temp.
5: methanol; CCl4
With potassium tert-butylate; methyllithium; toluene-4-sulfonic acid; toluene-4-sulfonic acid; In methanol; tetrachloromethane; diethyl ether; pentane;
Guidance literature:
Multi-step reaction with 2 steps
1: diluted alcohol
With ethanol;
Guidance literature:
Multi-step reaction with 2 steps
1: hexamethylphosphoramide / diethyl ether; tetrahydrofuran / 1.) -65 deg C, 1.5 h, 2.) RT, overnight
2: methanol; CCl4
With N,N,N,N,N,N-hexamethylphosphoric triamide; In tetrahydrofuran; methanol; tetrachloromethane; diethyl ether;
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